Incidental Mutation 'IGL00090:Pou2f1'
ID |
1945 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Pou2f1
|
Ensembl Gene |
ENSMUSG00000026565 |
Gene Name |
POU domain, class 2, transcription factor 1 |
Synonyms |
Oct-1z, Oct-1A, Oct-1B, Oct-1C, oct-1, Oct1, 2810482H01Rik, Otf-1, Otf1 |
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
IGL00090
|
Quality Score |
|
Status
|
|
Chromosome |
1 |
Chromosomal Location |
165692723-165830247 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to T
at 165729867 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Serine
at position 162
(R162S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000125371
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027850]
[ENSMUST00000069609]
[ENSMUST00000111426]
[ENSMUST00000111427]
[ENSMUST00000111429]
[ENSMUST00000160260]
[ENSMUST00000160908]
[ENSMUST00000184643]
[ENSMUST00000159212]
|
AlphaFold |
no structure available at present |
Predicted Effect |
unknown
Transcript: ENSMUST00000027850
AA Change: R215S
|
SMART Domains |
Protein: ENSMUSP00000027850 Gene: ENSMUSG00000026565 AA Change: R215S
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
22 |
N/A |
INTRINSIC |
low complexity region
|
94 |
123 |
N/A |
INTRINSIC |
low complexity region
|
137 |
152 |
N/A |
INTRINSIC |
low complexity region
|
171 |
192 |
N/A |
INTRINSIC |
low complexity region
|
199 |
217 |
N/A |
INTRINSIC |
POU
|
241 |
315 |
1.55e-52 |
SMART |
low complexity region
|
316 |
332 |
N/A |
INTRINSIC |
HOX
|
342 |
404 |
2.54e-19 |
SMART |
low complexity region
|
422 |
448 |
N/A |
INTRINSIC |
low complexity region
|
453 |
520 |
N/A |
INTRINSIC |
low complexity region
|
529 |
567 |
N/A |
INTRINSIC |
low complexity region
|
675 |
685 |
N/A |
INTRINSIC |
low complexity region
|
688 |
705 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000069609
AA Change: R267S
|
SMART Domains |
Protein: ENSMUSP00000064000 Gene: ENSMUSG00000026565 AA Change: R267S
Domain | Start | End | E-Value | Type |
low complexity region
|
83 |
112 |
N/A |
INTRINSIC |
low complexity region
|
130 |
172 |
N/A |
INTRINSIC |
low complexity region
|
189 |
204 |
N/A |
INTRINSIC |
low complexity region
|
223 |
244 |
N/A |
INTRINSIC |
low complexity region
|
251 |
269 |
N/A |
INTRINSIC |
POU
|
293 |
367 |
1.55e-52 |
SMART |
low complexity region
|
368 |
384 |
N/A |
INTRINSIC |
HOX
|
394 |
456 |
2.54e-19 |
SMART |
low complexity region
|
474 |
500 |
N/A |
INTRINSIC |
low complexity region
|
505 |
572 |
N/A |
INTRINSIC |
low complexity region
|
581 |
619 |
N/A |
INTRINSIC |
low complexity region
|
727 |
737 |
N/A |
INTRINSIC |
low complexity region
|
740 |
757 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000082225
|
SMART Domains |
Protein: ENSMUSP00000080856 Gene: ENSMUSG00000026565
Domain | Start | End | E-Value | Type |
low complexity region
|
83 |
112 |
N/A |
INTRINSIC |
low complexity region
|
130 |
172 |
N/A |
INTRINSIC |
low complexity region
|
189 |
204 |
N/A |
INTRINSIC |
POU
|
233 |
309 |
4.88e-27 |
SMART |
low complexity region
|
310 |
326 |
N/A |
INTRINSIC |
HOX
|
336 |
398 |
2.54e-19 |
SMART |
low complexity region
|
416 |
442 |
N/A |
INTRINSIC |
low complexity region
|
447 |
514 |
N/A |
INTRINSIC |
low complexity region
|
523 |
561 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111426
AA Change: R267S
PolyPhen 2
Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000107055 Gene: ENSMUSG00000026565 AA Change: R267S
Domain | Start | End | E-Value | Type |
low complexity region
|
83 |
112 |
N/A |
INTRINSIC |
low complexity region
|
130 |
172 |
N/A |
INTRINSIC |
low complexity region
|
189 |
204 |
N/A |
INTRINSIC |
low complexity region
|
223 |
244 |
N/A |
INTRINSIC |
low complexity region
|
251 |
269 |
N/A |
INTRINSIC |
POU
|
293 |
367 |
6.7e-55 |
SMART |
low complexity region
|
368 |
384 |
N/A |
INTRINSIC |
HOX
|
394 |
456 |
1.3e-21 |
SMART |
low complexity region
|
474 |
500 |
N/A |
INTRINSIC |
low complexity region
|
531 |
596 |
N/A |
INTRINSIC |
low complexity region
|
605 |
643 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000111427
AA Change: R267S
|
SMART Domains |
Protein: ENSMUSP00000107056 Gene: ENSMUSG00000026565 AA Change: R267S
Domain | Start | End | E-Value | Type |
low complexity region
|
83 |
112 |
N/A |
INTRINSIC |
low complexity region
|
130 |
172 |
N/A |
INTRINSIC |
low complexity region
|
189 |
204 |
N/A |
INTRINSIC |
low complexity region
|
223 |
244 |
N/A |
INTRINSIC |
low complexity region
|
251 |
269 |
N/A |
INTRINSIC |
POU
|
293 |
367 |
1.55e-52 |
SMART |
low complexity region
|
368 |
384 |
N/A |
INTRINSIC |
HOX
|
394 |
456 |
2.54e-19 |
SMART |
low complexity region
|
474 |
500 |
N/A |
INTRINSIC |
low complexity region
|
531 |
596 |
N/A |
INTRINSIC |
low complexity region
|
605 |
643 |
N/A |
INTRINSIC |
low complexity region
|
751 |
761 |
N/A |
INTRINSIC |
low complexity region
|
764 |
781 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000111429
AA Change: R255S
|
SMART Domains |
Protein: ENSMUSP00000107057 Gene: ENSMUSG00000026565 AA Change: R255S
Domain | Start | End | E-Value | Type |
low complexity region
|
71 |
100 |
N/A |
INTRINSIC |
low complexity region
|
118 |
160 |
N/A |
INTRINSIC |
low complexity region
|
177 |
192 |
N/A |
INTRINSIC |
low complexity region
|
211 |
232 |
N/A |
INTRINSIC |
low complexity region
|
239 |
257 |
N/A |
INTRINSIC |
POU
|
281 |
355 |
6.7e-55 |
SMART |
low complexity region
|
356 |
372 |
N/A |
INTRINSIC |
HOX
|
382 |
444 |
1.3e-21 |
SMART |
low complexity region
|
462 |
488 |
N/A |
INTRINSIC |
low complexity region
|
493 |
560 |
N/A |
INTRINSIC |
low complexity region
|
569 |
607 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000160260
AA Change: R278S
|
SMART Domains |
Protein: ENSMUSP00000124738 Gene: ENSMUSG00000026565 AA Change: R278S
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
22 |
N/A |
INTRINSIC |
low complexity region
|
94 |
123 |
N/A |
INTRINSIC |
low complexity region
|
141 |
183 |
N/A |
INTRINSIC |
low complexity region
|
200 |
215 |
N/A |
INTRINSIC |
low complexity region
|
234 |
255 |
N/A |
INTRINSIC |
low complexity region
|
262 |
280 |
N/A |
INTRINSIC |
POU
|
304 |
378 |
1.55e-52 |
SMART |
low complexity region
|
379 |
395 |
N/A |
INTRINSIC |
HOX
|
405 |
467 |
2.54e-19 |
SMART |
low complexity region
|
485 |
511 |
N/A |
INTRINSIC |
low complexity region
|
542 |
607 |
N/A |
INTRINSIC |
low complexity region
|
616 |
654 |
N/A |
INTRINSIC |
low complexity region
|
762 |
772 |
N/A |
INTRINSIC |
low complexity region
|
775 |
792 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000160908
AA Change: R278S
|
SMART Domains |
Protein: ENSMUSP00000125444 Gene: ENSMUSG00000026565 AA Change: R278S
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
22 |
N/A |
INTRINSIC |
low complexity region
|
94 |
123 |
N/A |
INTRINSIC |
low complexity region
|
141 |
183 |
N/A |
INTRINSIC |
low complexity region
|
200 |
215 |
N/A |
INTRINSIC |
low complexity region
|
234 |
255 |
N/A |
INTRINSIC |
low complexity region
|
262 |
280 |
N/A |
INTRINSIC |
POU
|
304 |
378 |
1.55e-52 |
SMART |
low complexity region
|
379 |
395 |
N/A |
INTRINSIC |
HOX
|
405 |
467 |
2.54e-19 |
SMART |
low complexity region
|
485 |
511 |
N/A |
INTRINSIC |
low complexity region
|
516 |
583 |
N/A |
INTRINSIC |
low complexity region
|
592 |
630 |
N/A |
INTRINSIC |
low complexity region
|
738 |
748 |
N/A |
INTRINSIC |
low complexity region
|
751 |
768 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000184643
AA Change: R255S
|
SMART Domains |
Protein: ENSMUSP00000138962 Gene: ENSMUSG00000026565 AA Change: R255S
Domain | Start | End | E-Value | Type |
low complexity region
|
71 |
100 |
N/A |
INTRINSIC |
low complexity region
|
118 |
160 |
N/A |
INTRINSIC |
low complexity region
|
177 |
192 |
N/A |
INTRINSIC |
low complexity region
|
211 |
232 |
N/A |
INTRINSIC |
low complexity region
|
239 |
257 |
N/A |
INTRINSIC |
POU
|
281 |
355 |
6.7e-55 |
SMART |
low complexity region
|
356 |
372 |
N/A |
INTRINSIC |
HOX
|
382 |
444 |
1.3e-21 |
SMART |
low complexity region
|
462 |
488 |
N/A |
INTRINSIC |
low complexity region
|
493 |
560 |
N/A |
INTRINSIC |
low complexity region
|
569 |
607 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000159212
AA Change: R162S
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000125371 Gene: ENSMUSG00000026565 AA Change: R162S
Domain | Start | End | E-Value | Type |
low complexity region
|
71 |
100 |
N/A |
INTRINSIC |
low complexity region
|
118 |
160 |
N/A |
INTRINSIC |
low complexity region
|
177 |
192 |
N/A |
INTRINSIC |
low complexity region
|
211 |
232 |
N/A |
INTRINSIC |
low complexity region
|
239 |
257 |
N/A |
INTRINSIC |
POU
|
281 |
355 |
1.55e-52 |
SMART |
low complexity region
|
356 |
372 |
N/A |
INTRINSIC |
HOX
|
382 |
444 |
2.54e-19 |
SMART |
low complexity region
|
462 |
488 |
N/A |
INTRINSIC |
low complexity region
|
493 |
560 |
N/A |
INTRINSIC |
low complexity region
|
569 |
607 |
N/A |
INTRINSIC |
low complexity region
|
715 |
725 |
N/A |
INTRINSIC |
low complexity region
|
728 |
745 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000177472
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000176942
|
SMART Domains |
Protein: ENSMUSP00000135052 Gene: ENSMUSG00000026565
Domain | Start | End | E-Value | Type |
low complexity region
|
65 |
94 |
N/A |
INTRINSIC |
low complexity region
|
112 |
154 |
N/A |
INTRINSIC |
low complexity region
|
171 |
186 |
N/A |
INTRINSIC |
low complexity region
|
205 |
226 |
N/A |
INTRINSIC |
low complexity region
|
233 |
251 |
N/A |
INTRINSIC |
POU
|
275 |
349 |
1.55e-52 |
SMART |
low complexity region
|
350 |
366 |
N/A |
INTRINSIC |
HOX
|
376 |
438 |
2.54e-19 |
SMART |
low complexity region
|
456 |
482 |
N/A |
INTRINSIC |
low complexity region
|
487 |
554 |
N/A |
INTRINSIC |
low complexity region
|
563 |
601 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The OCT1 transcription factor was among the first identified members of the POU transcription factor family (summarized by Sturm et al., 1993 [PubMed 8314572]). Members of this family contain the POU domain, a 160-amino acid region necessary for DNA binding to the octameric sequence ATGCAAAT.[supplied by OMIM, Jul 2010] PHENOTYPE: Homozygous mutation of this gene results in prenatal lethality, with earlier lethality on either a 129/Sv or C57BL/6 background than a mixed 129/Sv and C57BL/6 background. Embryos show decreased erythropoiesis and partial penetrance of small lens size. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb5 |
T |
C |
12: 118,854,345 (GRCm39) |
T857A |
probably benign |
Het |
Abcc9 |
A |
T |
6: 142,578,916 (GRCm39) |
|
probably benign |
Het |
Adam11 |
A |
G |
11: 102,667,657 (GRCm39) |
T709A |
probably benign |
Het |
Adgre1 |
A |
G |
17: 57,757,055 (GRCm39) |
I771V |
probably benign |
Het |
Adgrv1 |
T |
G |
13: 81,553,527 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
C |
T |
13: 81,726,220 (GRCm39) |
D602N |
probably damaging |
Het |
Adra1d |
G |
T |
2: 131,403,597 (GRCm39) |
D164E |
possibly damaging |
Het |
Ago3 |
A |
G |
4: 126,265,334 (GRCm39) |
L319P |
probably damaging |
Het |
Aim2 |
A |
G |
1: 173,283,031 (GRCm39) |
S38G |
probably benign |
Het |
Apoh |
A |
G |
11: 108,286,660 (GRCm39) |
D28G |
probably benign |
Het |
Atm |
C |
T |
9: 53,435,743 (GRCm39) |
R189K |
probably damaging |
Het |
Bbs1 |
T |
C |
19: 4,943,038 (GRCm39) |
T451A |
probably benign |
Het |
BC034090 |
T |
C |
1: 155,101,193 (GRCm39) |
D719G |
possibly damaging |
Het |
Bcr |
T |
C |
10: 74,992,903 (GRCm39) |
|
probably benign |
Het |
Bmp2 |
A |
T |
2: 133,402,947 (GRCm39) |
Q166L |
probably benign |
Het |
Bms1 |
A |
T |
6: 118,381,544 (GRCm39) |
S665T |
probably benign |
Het |
Ccser1 |
A |
T |
6: 62,357,126 (GRCm39) |
T855S |
possibly damaging |
Het |
Cfap36 |
C |
T |
11: 29,172,875 (GRCm39) |
V217M |
probably benign |
Het |
Clca3b |
T |
C |
3: 144,542,393 (GRCm39) |
N470D |
probably damaging |
Het |
Cort |
A |
G |
4: 149,209,752 (GRCm39) |
F100S |
probably damaging |
Het |
Cyp4f14 |
G |
T |
17: 33,133,540 (GRCm39) |
D105E |
probably benign |
Het |
Dnah1 |
A |
G |
14: 31,009,830 (GRCm39) |
S1913P |
probably benign |
Het |
Fam91a1 |
A |
T |
15: 58,302,584 (GRCm39) |
H308L |
probably damaging |
Het |
Fbn1 |
A |
C |
2: 125,166,867 (GRCm39) |
I2016M |
probably damaging |
Het |
Fibcd1 |
T |
A |
2: 31,723,886 (GRCm39) |
Q251L |
possibly damaging |
Het |
Flg2 |
T |
A |
3: 93,109,416 (GRCm39) |
Y481* |
probably null |
Het |
Ly9 |
A |
T |
1: 171,421,019 (GRCm39) |
I624N |
probably damaging |
Het |
Mapt |
C |
T |
11: 104,213,311 (GRCm39) |
S301L |
probably damaging |
Het |
Meiob |
G |
A |
17: 25,042,603 (GRCm39) |
V144I |
probably benign |
Het |
Muc4 |
G |
A |
16: 32,754,086 (GRCm38) |
G1321R |
probably benign |
Het |
Myo5a |
T |
A |
9: 75,068,779 (GRCm39) |
C660* |
probably null |
Het |
Necab3 |
G |
T |
2: 154,389,488 (GRCm39) |
|
probably benign |
Het |
Nr2c2ap |
A |
G |
8: 70,585,279 (GRCm39) |
Y93C |
probably damaging |
Het |
Nxpe5 |
A |
G |
5: 138,247,096 (GRCm39) |
D356G |
probably benign |
Het |
Or10ak9 |
T |
A |
4: 118,726,484 (GRCm39) |
Y168N |
probably damaging |
Het |
Or2w25 |
A |
T |
11: 59,504,147 (GRCm39) |
Y119F |
possibly damaging |
Het |
Plce1 |
A |
G |
19: 38,734,232 (GRCm39) |
Q1544R |
probably damaging |
Het |
Plppr4 |
T |
A |
3: 117,115,869 (GRCm39) |
T605S |
probably benign |
Het |
Poglut1 |
C |
A |
16: 38,363,278 (GRCm39) |
W167L |
possibly damaging |
Het |
Ptprf |
A |
G |
4: 118,080,417 (GRCm39) |
|
probably benign |
Het |
Reln |
C |
A |
5: 22,244,563 (GRCm39) |
G805V |
possibly damaging |
Het |
Rexo2 |
A |
G |
9: 48,385,747 (GRCm39) |
S126P |
probably damaging |
Het |
Robo4 |
A |
G |
9: 37,322,400 (GRCm39) |
S844G |
probably damaging |
Het |
Scn7a |
A |
G |
2: 66,513,671 (GRCm39) |
|
probably benign |
Het |
Sdc1 |
A |
G |
12: 8,840,459 (GRCm39) |
T75A |
possibly damaging |
Het |
Slc38a4 |
C |
T |
15: 96,917,690 (GRCm39) |
E12K |
probably benign |
Het |
Spata31h1 |
T |
G |
10: 82,119,586 (GRCm39) |
M4475L |
probably benign |
Het |
Tbck |
T |
C |
3: 132,448,854 (GRCm39) |
|
probably null |
Het |
Tex2 |
A |
T |
11: 106,459,361 (GRCm39) |
V23E |
probably damaging |
Het |
Zfp770 |
A |
G |
2: 114,026,413 (GRCm39) |
V552A |
probably benign |
Het |
Zfyve26 |
T |
C |
12: 79,296,234 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Pou2f1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Pou2f1
|
APN |
1 |
165,724,159 (GRCm39) |
splice site |
probably benign |
|
IGL01627:Pou2f1
|
APN |
1 |
165,708,002 (GRCm39) |
unclassified |
probably benign |
|
IGL01707:Pou2f1
|
APN |
1 |
165,742,685 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02735:Pou2f1
|
APN |
1 |
165,703,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02740:Pou2f1
|
APN |
1 |
165,710,685 (GRCm39) |
nonsense |
probably null |
|
IGL03117:Pou2f1
|
APN |
1 |
165,762,382 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03272:Pou2f1
|
APN |
1 |
165,724,049 (GRCm39) |
missense |
possibly damaging |
0.67 |
R0021:Pou2f1
|
UTSW |
1 |
165,703,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R1437:Pou2f1
|
UTSW |
1 |
165,719,399 (GRCm39) |
missense |
probably damaging |
0.98 |
R2171:Pou2f1
|
UTSW |
1 |
165,707,925 (GRCm39) |
unclassified |
probably benign |
|
R3722:Pou2f1
|
UTSW |
1 |
165,722,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R3789:Pou2f1
|
UTSW |
1 |
165,722,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R3790:Pou2f1
|
UTSW |
1 |
165,722,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R3901:Pou2f1
|
UTSW |
1 |
165,722,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R4225:Pou2f1
|
UTSW |
1 |
165,738,889 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4459:Pou2f1
|
UTSW |
1 |
165,722,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R4460:Pou2f1
|
UTSW |
1 |
165,722,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R4573:Pou2f1
|
UTSW |
1 |
165,740,830 (GRCm39) |
missense |
probably benign |
0.29 |
R4820:Pou2f1
|
UTSW |
1 |
165,719,517 (GRCm39) |
intron |
probably benign |
|
R4838:Pou2f1
|
UTSW |
1 |
165,744,492 (GRCm39) |
missense |
probably null |
1.00 |
R5579:Pou2f1
|
UTSW |
1 |
165,742,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R5856:Pou2f1
|
UTSW |
1 |
165,742,699 (GRCm39) |
missense |
probably benign |
0.14 |
R5951:Pou2f1
|
UTSW |
1 |
165,710,625 (GRCm39) |
unclassified |
probably benign |
|
R6128:Pou2f1
|
UTSW |
1 |
165,703,056 (GRCm39) |
unclassified |
probably benign |
|
R6145:Pou2f1
|
UTSW |
1 |
165,703,002 (GRCm39) |
unclassified |
probably benign |
|
R6216:Pou2f1
|
UTSW |
1 |
165,707,889 (GRCm39) |
unclassified |
probably benign |
|
R6971:Pou2f1
|
UTSW |
1 |
165,759,258 (GRCm39) |
missense |
probably damaging |
0.98 |
R7052:Pou2f1
|
UTSW |
1 |
165,742,684 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7403:Pou2f1
|
UTSW |
1 |
165,738,955 (GRCm39) |
missense |
unknown |
|
R7404:Pou2f1
|
UTSW |
1 |
165,738,955 (GRCm39) |
missense |
unknown |
|
R7741:Pou2f1
|
UTSW |
1 |
165,703,444 (GRCm39) |
missense |
probably damaging |
0.98 |
R8011:Pou2f1
|
UTSW |
1 |
165,722,472 (GRCm39) |
critical splice donor site |
probably null |
|
R8478:Pou2f1
|
UTSW |
1 |
165,759,287 (GRCm39) |
start codon destroyed |
probably null |
|
R8804:Pou2f1
|
UTSW |
1 |
165,708,039 (GRCm39) |
missense |
unknown |
|
R8892:Pou2f1
|
UTSW |
1 |
165,708,027 (GRCm39) |
missense |
unknown |
|
R9126:Pou2f1
|
UTSW |
1 |
165,722,603 (GRCm39) |
missense |
unknown |
|
R9151:Pou2f1
|
UTSW |
1 |
165,703,640 (GRCm39) |
intron |
probably benign |
|
R9469:Pou2f1
|
UTSW |
1 |
165,740,830 (GRCm39) |
missense |
probably benign |
0.29 |
R9665:Pou2f1
|
UTSW |
1 |
165,703,600 (GRCm39) |
missense |
probably damaging |
0.99 |
RF012:Pou2f1
|
UTSW |
1 |
165,740,800 (GRCm39) |
missense |
unknown |
|
X0022:Pou2f1
|
UTSW |
1 |
165,724,025 (GRCm39) |
nonsense |
probably null |
|
|
Posted On |
2011-07-12 |